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Nathan Fischel-Ghodsian

Showing results (1-10 of 28) with videos related to

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The New England Journal of Medicine|September 26, 2003
Mitochondrial diseasesNathan Fischel-Ghodsian
Ear and Hearing|August 19, 2003
Mitochondrial deafnessNathan Fischel-Ghodsian
Pharmacogenomics|February 23, 2005
Genetic factors in aminoglycoside toxicityNathan Fischel-Ghodsian
American Journal of Medical Genetics. Part A|February 26, 2004
Mitochondrial myopathy and sideroblastic anemiaKari A Casas, Nathan Fischel-Ghodsian
Molecular Genetics and Metabolism|June 2, 2009
Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteinsYelena Bykhovskaya, Emebet Mengesha, Nathan Fischel-Ghodsian
Molecular Genetics and Metabolism|March 22, 2007
Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA)Yelena Bykhovskaya, Emebet Mengesha, Nathan Fischel-Ghodsian
Mitochondrion|August 27, 2005
Mitochondrial dysfunction in hearing lossNathan Fischel-Ghodsian, Richard D Kopke, Xianxi Ge
RNA (New York, N.Y.)|July 24, 2008
Partial activity is seen with many substitutions of highly conserved active site residues in human Pseudouridine synthase 1Bryan S Sibert, Nathan Fischel-Ghodsian, Jeffrey R Patton
BMC Medical Genetics|December 25, 2007
MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA geneEster Ballana, Josep Maria Mercader, Nathan Fischel-Ghodsian, et al.
American Journal of Human Genetics|April 27, 2004
Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA)Yelena Bykhovskaya, Kari Casas, Emebet Mengesha, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
The New England Journal of Medicine|September 26, 2003
Mitochondrial diseasesNathan Fischel-Ghodsian
Ear and Hearing|August 19, 2003
Mitochondrial deafnessNathan Fischel-Ghodsian
Pharmacogenomics|February 23, 2005
Genetic factors in aminoglycoside toxicityNathan Fischel-Ghodsian
American Journal of Medical Genetics. Part A|February 26, 2004
Mitochondrial myopathy and sideroblastic anemiaKari A Casas, Nathan Fischel-Ghodsian
Molecular Genetics and Metabolism|June 2, 2009
Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteinsYelena Bykhovskaya, Emebet Mengesha, Nathan Fischel-Ghodsian
Molecular Genetics and Metabolism|March 22, 2007
Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA)Yelena Bykhovskaya, Emebet Mengesha, Nathan Fischel-Ghodsian
Mitochondrion|August 27, 2005
Mitochondrial dysfunction in hearing lossNathan Fischel-Ghodsian, Richard D Kopke, Xianxi Ge
RNA (New York, N.Y.)|July 24, 2008
Partial activity is seen with many substitutions of highly conserved active site residues in human Pseudouridine synthase 1Bryan S Sibert, Nathan Fischel-Ghodsian, Jeffrey R Patton
BMC Medical Genetics|December 25, 2007
MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA geneEster Ballana, Josep Maria Mercader, Nathan Fischel-Ghodsian, et al.
American Journal of Human Genetics|April 27, 2004
Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA)Yelena Bykhovskaya, Kari Casas, Emebet Mengesha, et al.
Pageof 3